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      Electron Microscopic, Genetic and Protein Expression Analyses of Helicobacter acinonychis Strains from a Bengal Tiger

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          Abstract

          Colonization by Helicobacter species is commonly noted in many mammals. These infections often remain unrecognized, but can cause severe health complications or more subtle host immune perturbations. The aim of this study was to isolate and characterize putative novel Helicobacter spp. from Bengal tigers in Thailand. Morphological investigation (Gram-staining and electron microscopy) and genetic studies (16SrRNA, 23SrRNA, flagellin, urease and prophage gene analyses, RAPD DNA fingerprinting and restriction fragment polymorphisms) as well as Western blotting were used to characterize the isolated Helicobacters. Electron microscopy revealed spiral-shaped bacteria, which varied in length (2.5–6 µm) and contained up to four monopolar sheathed flagella. The 16SrRNA, 23SrRNA, sequencing and protein expression analyses identified novel H. acinonychis isolates closely related to H. pylori. These Asian isolates are genetically very similar to H. acinonychis strains of other big cats (cheetahs, lions, lion-tiger hybrid and other tigers) from North America and Europe, which is remarkable in the context of the great genetic diversity among worldwide H. pylori strains. We also found by immunoblotting that the Bengal tiger isolates express UreaseA/B, flagellin, BabA adhesin, neutrophil-activating protein NapA, HtrA protease, γ-glutamyl-transpeptidase GGT, Slt lytic transglycosylase and two DNA transfer relaxase orthologs that were known from H. pylori, but not the cag pathogenicity island, nor CagA, VacA, SabA, DupA or OipA proteins. These results give fresh insights into H. acinonychis genetics and the expression of potential pathogenicity-associated factors and their possible pathophysiological relevance in related gastric infections.

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          Most cited references65

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          Unidentified curved bacilli on gastric epithelium in active chronic gastritis.

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            Nod1 responds to peptidoglycan delivered by the Helicobacter pylori cag pathogenicity island.

            Epithelial cells can respond to conserved bacterial products that are internalized after either bacterial invasion or liposome treatment of cells. We report here that the noninvasive Gram-negative pathogen Helicobacter pylori was recognized by epithelial cells via Nod1, an intracellular pathogen-recognition molecule with specificity for Gram-negative peptidoglycan. Nod1 detection of H. pylori depended on the delivery of peptidoglycan to host cells by a bacterial type IV secretion system, encoded by the H. pylori cag pathogenicity island. Consistent with involvement of Nod1 in host defense, Nod1-deficient mice were more susceptible to infection by cag pathogenicity island-positive H. pylori than were wild-type mice. We propose that sensing of H. pylori by Nod1 represents a model for host recognition of noninvasive pathogens.
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              Helicobacter pylori adhesin binding fucosylated histo-blood group antigens revealed by retagging.

              The bacterium Helicobacter pylori is the causative agent for peptic ulcer disease. Bacterial adherence to the human gastric epithelial lining is mediated by the fucosylated Lewis b (Leb) histo-blood group antigen. The Leb-binding adhesin, BabA, was purified by receptor activity-directed affinity tagging. The bacterial Leb-binding phenotype was associated with the presence of the cag pathogenicity island among clinical isolates of H. pylori. A vaccine strategy based on the BabA adhesin might serve as a means to target the virulent type I strains of H. pylori.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                5 August 2013
                : 8
                : 8
                : e71220
                Affiliations
                [1 ]Institute of Medical Microbiology, Otto von Guericke University Magdeburg, Magdeburg, Germany
                [2 ]Helmholtz Centre for Infection Research, Braunschweig, Germany
                [3 ]Institute for Environmental Health, Inc., Seattle, Washington, United States of America
                [4 ]Institute for Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany
                [5 ]Centre for Innate Immunity & Infectious Diseases, Monash Institute of Medical Research, Clayton, Australia
                [6 ]Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America
                [7 ]Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, United States of America
                University of Osnabrueck, Germany
                Author notes

                Competing Interests: OAO is employed by Institute for Environmental Health Inc and declares no conflict of interest. This does not alter the authors’ adherence to all the PLOS ONE polices on sharing data and materials.

                Conceived and designed the experiments: NT FRT OAO MR SB. Performed the experiments: NT FRT OAO MR. Analyzed the data: NT FRT OAO MR DEB SB. Contributed reagents/materials/analysis tools: NL RLF JGF DEB WSB. Wrote the paper: NT SB. Made figures: NT FRT MR OAO SB.

                [¤a]

                Current address: Department of Biology, Chair of Microbiology, Friedrich Alexander University Erlangen-Nuremberg, Erlangen, Germany

                [¤b]

                Current address: Department of Medicine, University of California San Diego, San Diego, California, United States of America

                Article
                PONE-D-13-14264
                10.1371/journal.pone.0071220
                3733902
                23940723
                2c6eece1-525f-43a1-a925-049aeef845d8
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 4 April 2013
                : 26 June 2013
                Page count
                Pages: 14
                Funding
                The work of SB is supported through a DFG grant (project B10 of CRC-796). FRT was supported by a stipend of SENACYT (Secretaria Nacional de Ciencia y Tecnologia, Panama). RLF is a Senior Research Fellow of the NHMRC. Research at MIMR is supported by the Victorian Government’s Operational Infrastructure Support Program. The research in DB’s group has been supported by US National Institutes of Health Grants (R21 AI078237 and R21 AI088337). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Computational Biology
                Molecular Genetics
                Gene Expression
                Ecology
                Microbial Ecology
                Evolutionary Biology
                Evolutionary Systematics
                Taxonomy
                Microbial Taxonomy
                Microbiology
                Microbial Ecology
                Molecular Cell Biology
                Gene Expression
                Zoology
                Mammalogy
                Medicine
                Infectious Diseases
                Bacterial Diseases
                Helicobacter Pylori
                Veterinary Science
                Animal Types
                Large Animals

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                Uncategorized

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